81294 Mlh1 gene dup/delete variant
Pathology & Lab
Also known as: MLH1 copy number analysis, MLH1 deletion duplication testing
Mutator S Homolog 1 (MLH1) gene duplication and deletion variant analysis to identify copy number variations in Lynch syndrome.
Clinical Context
Detects MLH1 deletions and duplications accounting for 10-15% of Lynch syndrome cases, improving diagnostic yield when sequencing is negative.
RVU Breakdown
| Work RVU | 0.00 |
| Practice Expense RVU | 0.00 |
| Malpractice RVU | 0.00 |
| Total RVU | 0.00 |
Specialties
Track This Code in RVU Edge
Log procedures, calculate wRVUs, and benchmark against MGMA data — all in one app.
CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.